Martin Chevarin
13PUBLICATIONS
74CO-AUTHORS
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Publications (13)
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|Oct 23, 2025
PERIGENOMED-CLINICS 1-the first study on feasibility, acceptability and psychosocial impact of PERIGENOMED: a pilot project aimed at providing initial concrete evidence on the relevance of panel-based genome sequencing for newborn screening (NBS) in France.Camille Level, Christel Thauvin-Robinet, Christine Binquet
|Apr 16, 2024
Clinical phenotype of the PIK3R1-related vascular overgrowth syndrome.Paul Kuentz, Camille Engel, Mathieu Laeng
|Nov 17, 2023
Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples.Robin Wijngaard, German Demidov, Luke O'Gorman
|Oct 18, 2023
Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples.Robin Wijngaard, German Demidov, Luke O'Gorman
|Nov 30, 2022
A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort.Philippine Garret, Martin Chevarin, Antonio Vitobello
|Aug 26, 2022
Evaluation of Next-Generation Sequencing Applied to Cryptosporidium parvum and Cryptosporidium hominis Epidemiological Study.Eloïse Bailly, Stéphane Valot, Anne Vincent
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Frequent Collaborators
5 joint publications
Paul Kuentz
5 joint publications
Antonio Vitobello
4 joint publications
Julien Thevenon
4 joint publications
Anne-Sophie Denommé-Pichon
3 joint publications
Christophe Philippe
3 joint publications
Christel Thauvin-Robinet
3 joint publications
Ange-Line Bruel
3 joint publications
Laurence Faivre
2 joint publications
Pierre Vabres
2 joint publications
Sébastien Moutton
